4.5 Article

Unlocking the effect of Zn2+ on crystal structure, optical properties, and photocatalytic degradation of perfluoroalkyl substances (PFAS) of Bi2WO6

Journal

ENVIRONMENTAL SCIENCE-WATER RESEARCH & TECHNOLOGY
Volume 9, Issue 11, Pages 2866-2879

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ew00430a

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In this study, the photocatalytic activity of bismuth tungstate (Bi2WO6) for the degradation of perfluoroalkyl substances (PFAS) was enhanced by partially substituting Zn2+ for Bi3+ in the crystal lattice. The partial substitution of Zn2+ influenced the crystal structure, optical properties, and morphology of the nanoparticles of Bi2WO6, resulting in enhanced photocatalytic activity. The photodegradation of PFAS was mainly attributed to the photo-excited holes and superoxide radicals generated during the process.
Bismuth tungstate (Bi2WO6) with a layered structure and visible light response exhibits excellent photocatalytic activity. To enhance its photocatalytic activity for the degradation of perfluoroalkyl substances (PFAS), Zn2+ is partially substituted for Bi3+ in the Bi2WO6 lattice in this study. Particularly, the effect of Zn2+ content (0-22.5 at%) on the crystal structure, optical property, and photocatalytic activity for the photodegradation of PFAS of Bi2WO6 is investigated. According to the Le Bail fits, the unit-cell volume is slightly reduced from 487.7 angstrom(3) to 480.8 angstrom(3) by the partial substitution of smaller Zn-2+ (0.74 angstrom for CN = 6) for larger Bi3+ (1.03 A for CN = 6) in the Bi2WO6 crystal lattice, and the solubility of Zn2+ in the Bi2WO6 lattice is found to be below 17.5 at%. The partial substitution of Zn2+ influences the self-aggregation of nanoparticles, Ostwald ripening, and self-organization of nanoplates, resulting in different morphologies. Although the optical bandgap energy of Bi2WO6 is not significantly altered upon the partial substitution of Zn2+, the conduction and valence bands simultaneously shift upward. Among the Bi2-xZnxWO6+delta photocatalysts, 2.5 at% Zn2+-substituted Bi2WO6 exhibits larger water oxidation photocurrent density (0.316 mA cm(-2) at 1.23 V-RHE) and the highest photocatalytic activity for the photodegradation of PFH(x)A (k(1) = 0.012 min(-1)). The trapping experiments confirm that the photo-excited holes (h(+)) and superoxide radicals (O-2(center dot-)) are the major reactive species involved in the photodegradation of PFH(x)A. Liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF/MS) reveals that decarboxylation and defluorination are the main possible routes for the photodegradation of PFH(x)A over Bi2-xZnxWO6+delta photocatalysts. Our findings suggest that the partial Zn2+-to-Bi2+ substitution can enhance the photocatalytic activity of Bi2WO6 for the degradation of PFAS.

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